Evaluation of the Biodistribution of Mesenchymal Stem Cells in a Pre-clinical Renal Tuberculosis Model by Non-linear Magnetic Response Measurements
Bone-marrow derived mesenchymal stem cells (MSCs) exert anti-tuberculosis effects due to their potential to repair damaged tissues and modulate inflammatory immune responses. MSCs were reported to be recruited to the Mycobacterium tuberculosis (Mtb) affected sites in the organism. However, due to li...
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Veröffentlicht in: | Frontiers in physics 2021-04, Vol.9 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Bone-marrow derived mesenchymal stem cells (MSCs) exert anti-tuberculosis effects due to their potential to repair damaged tissues and modulate inflammatory immune responses. MSCs were reported to be recruited to the
Mycobacterium tuberculosis (Mtb)
affected sites in the organism. However, due to limitations of presently applied
in vivo
imaging techniques the trafficking and biodistribution of MSCs in
Mtb
-infected organisms is not possible. In the current study MSCs were labeled with superparamagnetic iron oxide nanoparticles (SPIONs) as a negative MR contrast agent for imaging the biodistribution of MSCs
in vivo
. Trafficking of SPIONs-labeled MSCs was analyzed in a preclinical model of renal tuberculosis in male Chinchilla rabbits (
n
= 18) following intravenous administration on the days 0, 2, 3, and 7 employing a highly sensitive method of non-linear longitudinal magnetic response (NLR-M
2
) measurements. Within 48 h after injection, nanoparticle-labeled MSCs accumulated predominantly in lung, spleen, liver tissues, and paratracheal lymph nodes with subsequent decrease over the observation period of 7 days. The recruitment of MSCs to
Mtb
-affected organs was further proven by immunohistological analysis. NLR-M
2
allowed the detection of SPIONs-labeled cells at low concentrations in different organs and tissues giving insights of
in vivo
mesenchymal stem cells trafficking in organism after TB infection. |
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ISSN: | 2296-424X 2296-424X |
DOI: | 10.3389/fphy.2021.625622 |